Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Venturini, A."'
Autor:
Eclair Venturini Filho, Mariana K. Antoniazi, Rafael Q. Ferreira, Gabriel F. S. dos Santos, Claudia Pessoa, Celina J. Guimarães, José B. Vieira Neto, Artur M. S. Silva, Sandro J. Greco
Publikováno v:
European Journal of Organic Chemistry. 2022
Autor:
Eclair Venturini Filho, Mariana K. Antoniazi, Rafael Q. Ferreira, Gabriel F. S. dos Santos, Claudia Pessoa, Celina J. Guimarães, José B. Vieira Neto, Artur M. S. Silva, Sandro J. Greco
Publikováno v:
European Journal of Organic Chemistry. 2022
Autor:
Iemhoff, Andree, Vennewald, Maurice, Artz, Jens, Mebrahtu, Chalachew, Meledin, Alexander, Weirich, Thomas E., Hartmann, Heinrich, Besmehn, Astrid, Aramini, Matteo, Venturini, Federica, Mosselmans, Fred W., Held, Georg, Arrigo, Rosa, Palkovits, Regina
Publikováno v:
ChemCatChem 14(9), e202200179 (2022). doi:10.1002/cctc.202200179
Stabilization of single metal atoms is a persistent challenge in heterogeneous catalysis. Especially supported late transitions metals are prone to undergo agglomeration to nanoparticles under reducing conditions. In this study, nitrogen-rich covalen
Autor:
Bárbara C. Lemos, Eclair Venturini Filho, Rodolfo G. Fiorot, Fabrizio Medici, Sandro J. Greco, Maurizio Benaglia
Publikováno v:
European Journal of Organic Chemistry. 2022
Autor:
Gabriel G. Vargas, Roberta K. Rodrigues, Lucas Antônio Silveira Silva, Bruno Venturini Loureiro
Publikováno v:
Journal of Surfactants and Detergents. 23:21-40
Autor:
Eduam O. Boeira, Rodrigo dos Santos Fuscaldo, Pedro Henrique Vasconcelos Vontobel, Jessie Sobieski da Costa, Angélica Venturini Moro
Publikováno v:
European Journal of Organic Chemistry. 2019:2050-2055
Autor:
Manfred Erwin Schuster, John E. Proctor, Federica Venturini, Haosheng Feng, Jake M. Seymour, Simone Gallarati, Pilar Ferrer, David C. Grinter, Ivan da Silva, Rosa Arrigo, Georg Held, June Callison, Diego Gianolio
Unsupported and SiO2-supported Ni nanoparticles (NPs), were synthesised via hot-injection colloidal route using oleylamine (OAm) and trioctylphosphine (TOP) as reducing and protective agents, respectively. By adopting a multi-length scale structural
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7362bea1cfe90abe026bb1571b8cf0c9
https://usir.salford.ac.uk/id/eprint/56103/8/cctc.201901955.pdf
https://usir.salford.ac.uk/id/eprint/56103/8/cctc.201901955.pdf
Autor:
Mauro Panunzio, Elisa Bandini, Antonio D'Aurizio, Sha Long, Alessandro Venturini, Magda Monari
Publikováno v:
European journal of organic chemistry (Online) (2011): 6218–6225. doi:10.1002/ejoc.201100930
info:cnr-pdr/source/autori:Long, S. ; Monari, M. ; Panunzio, M.; Bandini, E. ; D'Aurizio, A.; Venturini, A./titolo:Hetero-Diels-Alder (HDA) Strategy for the Preparation of 6-Aryl-and Heteroaryl-Substituted Piperidin-2-one Scaffolds: Experimental and Theoretical Studies/doi:10.1002%2Fejoc.201100930/rivista:European journal of organic chemistry (Online)/anno:2011/pagina_da:6218/pagina_a:6225/intervallo_pagine:6218–6225/volume
info:cnr-pdr/source/autori:Long, S. ; Monari, M. ; Panunzio, M.; Bandini, E. ; D'Aurizio, A.; Venturini, A./titolo:Hetero-Diels-Alder (HDA) Strategy for the Preparation of 6-Aryl-and Heteroaryl-Substituted Piperidin-2-one Scaffolds: Experimental and Theoretical Studies/doi:10.1002%2Fejoc.201100930/rivista:European journal of organic chemistry (Online)/anno:2011/pagina_da:6218/pagina_a:6225/intervallo_pagine:6218–6225/volume
Preparation of piperidine-2-one scaffolds by the hetero-Diels-Alder (HAD) reaction, assisted by microwaves, is described. The versatility of this new approach has been demonstrated by the synthesis of racemic (+/-)-2-phenylpiperidine. Theoretical cal
Publikováno v:
European Journal of Organic Chemistry. 2012:3607-3616
Herein, we describe the total syntheses of three bioactive pyrones isolated from Polygala sabulosa (i.e., 1, 4, and 7) and eight isolated from Piper methysticum (i.e., 8–10, 13, 15, and 18–20) using the Heck–Matsuda arylation as the key strateg
Publikováno v:
European Journal of Organic Chemistry. 2011:7259-7270
The stereoselective synthesis of nitrogen analogues of biologically active isoaltholactone and goniothalesdiol are described. The successful strategy employed a Heck–Matsuda reaction between a chiral endocyclic enecarbamate bearing an ester functio